510(k) K930481

DENTAL CASTING ALLOY MODIFICATION-PF-4 by Deringer-Ney, Inc. — Product Code EJT

K930481 is an FDA 510(k) premarket notification submitted by Deringer-Ney, Inc. for the device "DENTAL CASTING ALLOY MODIFICATION-PF-4". The FDA issued a decision of Substantially Equivalent on March 31, 1993. The device falls under product code EJT (Alloy, Gold-Based Noble Metal), a Class II device regulated under 21 CFR 872.3060. Deringer-Ney, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 31, 1993
Date Received
January 29, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Alloy, Gold-Based Noble Metal
Device Class
Class II
Regulation Number
872.3060
Review Panel
DE
Submission Type